Liquid detergents containing a peptide trifluoromethyl ketone

ABSTRACT

Aqueous liquid detergent compositions are described which comprise a proteolytic enzyme wherein the proteolytic activity is reversibly inhibited by a peptide trifluoromethyl ketone.

FIELD OF THE INVENTION

This invention relates to liquid detergent compositions containingenzymes. More specifically, this invention pertains to liquid detergentcompositions containing a detersive surfactant, a proteolytic enzyme,and a peptide trifluoromethyl ketone.

BACKGROUND OF THE INVENTION

Protease-containing liquid aqueous detergents are well-known, especiallyin the context of laundry washing. A commonly encountered problem insuch protease-containing liquid aqueous detergents is the degradationphenomenon by the proteolytic enzyme of second enzymes in thecomposition, such as lipase, amylase and cellulase, or on the proteaseitself.

As a result, the stability of the second enzyme or the protease itselfin the detergent composition is affected and the detergent compositionconsequently performs less well.

In response to this problem, it has been proposed to use variousprotease inhibitors or stabilizers. For instance, U.S. Pat. No.4,566,985 proposes to use benzamidine hydrochloride, EP 376 705 proposesto use lower aliphatic alcohols or carboxylic acids, EP 381 262 proposesto use a mixture of a polyol and a boron compound, and co-pendingapplication EP 91870072.5 proposes to use aromatic borate esters.

It is thus an object of the present invention to provide otherreversible protease inhibitors which are effective and suitable for usein an aqueous liquid detergent composition.

In response to this object, the present invention proposes to usepeptide trifluoromethyl ketones as reversible protease inhibitors inaqueous liquid detergent compositions.

A particular advantage of the present invention is that peptidetrifluoromethyl ketones need only to be used at very low levels in theliquid detergent compositions herein. Thus several parts of materialsare made available for other ingredients. This is particularly criticalin the formulation of concentrated liquid detergent compositions whichare encompassed by the present invention.

Because the peptide trifluoromethyl ketones of the present ivnention areso efficient in inhibiting proteases, another advantage of the presentinvention is that even enzymes which are highly sensitive to proteolyticdegradation can now be incorporated in liquid detergent compositionscomprising a protease.

The use of peptide derivatives for the inhibition of proteins appears tohave been disclosed so far only in therapeutic applications. Forinstance, EP 293 881 discloses the use of peptide boronic acids asinhibitors of trypsin-like serine proteases. EP 185 390 and U.S. Pat.No. 4,399,065 disclose the use of certain peptide aldehydes derivativesfor the inhibition of blood coagulation. J 90029670 discloses the use ofoptically active alpha amino aldehydes for the inhibition of enzymes ingeneral. See also "Inhibition of Thrombin and Trypsin by TripeptideAldehydes", Int. J. Peptide Protein Res., Vol 12 (1978), pp. 217-221;Gaal, Bacsy & Rappay, and "Tripeptide Aldehyde Protease Inhibitors MayDepress in Vitro Prolactin and Growth Hromone Release" Endocrinology,Vol. 116, No. 4 (1985), pp. 1426-1432; Rappay, Makara, Bajusz & Nagy.Certain peptide trifluoromethyl ketones have been described asanti-inflammatory agents in co-pending U.S. application 07/780,607.Also, EP-A-473 502 discloses the use of peptide aldehydes to inhibitprotease-mediated skin irritation.

SUMMARY OF THE INVENTION

The present invention is a liquid aqueous detergent compositioncomprising:

from 1% to 80% of a detersive surfactant,

from 0.0001% to 1.0% of an active proteolytic enzyme or mixturesthereof,

characterized in that it further comprises from 0.00001% to 5% of apeptide trifluoromethyl ketone comprising from 2 to 50 amino acids, or amixture thereof.

DETAILED DESCRIPTION OF THE INVENTION

The liquid aqueous detergent compositions according to the presentinvention comprise three essential ingredients: (A) a peptidetrifluoromethyl ketone or a mixture thereof, (B) a proteolytic enzyme ora mixture thereof, and (C) a detersive surfactant. The compositionsaccording to the present invention preferably further comprise (D) adetergent-compatible second enzyme or a mixture thereof, and may furthercomprise (E) optional ingredients.

A. Peptides trifluoromethyl ketone

The detergent compositions according to the present invention comprise,as a first essential ingredient, a peptide trifluoromethyl ketonecomprising from 2 to 50 amino acids, or mixtures thereof. As usedherein, the term peptide trifluoromethyl ketone refers to compoundscomprising a peptidic chain wherein the C-terminal end of said chain isconverted from a carboxylic group to a trifluoromethyl ketone group.Peptide trifluoromethyl ketones are known per se and have been describedin the art, as well as processes for their manufacture. Preferredpeptide trifluoromethyl ketones for use herein comprise from 2 to 6amino acids, most preferably 3 to 4.

While not wanting to be bound by theory it is believed that the peptidetrifluoromethyl ketones according to the present invention bind to theproteolytic enzyme in the liquid detergent composition, therebyinhibiting said proteolytic enzyme. Upon dilution in water, theproteolytic activity is restored by dissociation of the proteolyticenzyme/peptide trifluoromethyl ketone complex.

The N-terminal end of said peptidic chain in the peptide trifluoromethylketone according to the present invention may be protected byappropriate protecting groups which are known to the man skilled in theart. However, in a highly preferred embodiment of the present invention,the N-terminal end of said peptidic chain is protected by a methylcarbamate (CH₃ O--(O)C--) or methyl urea (CH₃ N--(O)C--) group. Indeed,it has been found that peptide trifluoromethyl ketones according to thepresent invention which have methyl carbamate or methyl urea asN-terminal protecting groups are particularly stable, in that theefficiency of said protected peptide trifluoromethyl ketones ininhibiting proteolytic activity is better sustained throughout time,compared to unprotected or otherwise protected peptide trifluoromethylketones.

A particular advantage of the present invention is that it can betailored to each individual situation. Specifically, depending on theprotease which is used in a given detergent composition, peptidetrifluoromethyl ketones can be selected which are more effective thanothers in reversibly inhibiting said protease. Existing proteases can bedivided into trypsin, subtilisin, chymotrypsin and elastase -typeproteases. For trypsin-type proteases, suitable peptide trifluoromethylketones will include Lys-Ala-Lys(trifluoromethyl),Ile-Phe-Lys(trifluoromethyl), Phe-Pro-Arg(trifluoromethyl) and PheVal-Arg(trifluoromethyl). For subtilisin-type proteases, suitablepeptide trifluoromethyl ketones will includeLys-Ala-Ala(trifluoromethyl) Ala-Ala-Pro(trifluoromethyl),Gly-Ala-Leu(trifluoromethyl), Gly-Ala-Phe(trifluoromethyl),Phe-Gly-Ala-Leu(trifluoromethyl) and Phe-Gly-Ala-Phe(trifluoromethyl).For chymotrypsin-type proteases, suitable peptide trifluoromethylketones will include Leu-Leu-Phe(trifluoromethyl),Ala-Ala-Phe(trifluoromethyl) and Leu-Leu-Tyr(trifluoromethyl). ForElastase-type proteases, suitable peptide trifluoromethyl ketones willinclude Val-Pro-Val(trifluoromethyl) and Ala-Val-Leu(trifluoromethyl).

The preferred proteases for use in the detergent compositions which aredescribed in part B) hereinafter are subtilisin-type proteases. Thus,the preferred peptide trifluoromethyl ketones for use herein areLys-Ala-Ala(trifluoromethyl), Ala-Ala-Pro(trifluoromethyl),Gly-Ala-Leu(trifluoromethyl), Gly-Ala-Phe(trifluoromethyl),Phe-Gly-Ala-Leu(trifluoromethyl) and Phe-Gly-Ala-Phe(trifluoromethyl).Particularly preferred for use herein are Gly-Ala-Leu(trifluoromethyl)Gly-Ala-Phe(trifluoromethyl), Phe-Gly-Ala-Leu(trifluoromethyl) andPhe-Gly-Ala-Phe(trifluoromethyl) i.e. the N-terminal end of the peptidesis, respectively, Gly, Gly, Phe and Phe, and the C-terminal end of thepeptides is, respectively Leu, Phe, Leu and Phe. The carboxylic group ofthe Leu and Phe is converted to a trifluoromethyl ketone group.

All peptide trifluoromethyl ketones listed herein will of course bepreferably used in their methyl carbamate or methyl urea N-terminalprotected form. In the examples hereinafter a method is disclosed tosynthesize CH₃ O--(O)C-Phe-Gly-Ala-Leu(trifluoromethyl).

The compositions according to the present invention comprise from0.00001% to 5% by weight of the total composition of a peptidetrifluoromethyl ketone or mixtures thereof, preferably 0.0001% to 1%,most preferably from 0.0005% to 0.2%.

B. Proteolytic Enzyme

A second essential ingredient in the present liquid detergentcompositions is from about 0.0001 to 1.0, preferably about 0.0005 to0.2, most preferably about 0.002 to 0.1, weight % of active proteolyticenzyme. Mixtures of proteolytic enzyme are also included. Theproteolytic enzyme can be of animal, vegetable or microorganism(preferred) origin. Preferred for use herein are subtilisin-typeproteolytic enzymes. Particularly preferred is bacterial serineproteolytic enzyme obtained from Bacillus subtilis and/or Bacilluslicheniformis.

Suitable proteolytic enzymes include Novo Industri A/S Alcalas®(preferred), Esperas®, Savinas® (Copenhagen, Denmark), Gist-brocades'Maxatase®, Maxacal®, and Maxapem 15® (protein engineered Maxacal®)(Delft, Netherlands), and subtilisin BPN and BPN'(preferred), which arecommercially available. Preferred proteolytic enzymes are also modifiedbacterial serine proteases, such as those made by GenencorInternational, Inc.(San Francisco, Calif.) which are described inEuropean Patent Application Serial Number 87303761.8, filed Apr. 28,1987 (particularly pages 17, 24 and 98), and which is called herein"Protease B", and 199,404, Venegas, published Oct. 29, 1986, whichrefers to a modified bacterial serine proteolytic enzyme (GenencorInternational) which is called "Protease A" herein (same as BPN').Preferred proteolytic enzymes, then, are selected from the groupconsisting of Alcalase® (Novo Industri A/S), BPN', Protease A andProtease B (Genencor), and mixtures thereof. Protease B is mostpreferred.

C. Detersive Surfactant

From about 1 to 80, preferably about 5 to 50, most preferably about 10to 30, weight % of detersive surfactant is the third essentialingredient in the present invention. The detersive surfactant can beselected from the group consisting of anionics, nonionics, cationics,ampholytics, zwitterionics, and mixtures thereof. Although thecompositions according to the present invention are preferably used inthe context of Laundry cleaning, said compositions according to thepresent invention can be used in other different cleaning applicationsincluding hard surface cleaning, or dishwashing. The particularsurfactants used can therefore vary widely depending upon the particularend-use envisioned.

The benefits of the present invention are especially pronounced incompositions containing ingredients that are harsh to enzymes such ascertain detergency builders and surfactants. These, in general, include(but are not limited to anionic surfactants such as alkyl ether sulfatelinear alkyl benzene sulfonate, alkyl sulfate, etc. Suitable surfactantsare described below.

Anionic Surfactants

One type of anionic surfactant which can be utilized encompasses alkylester sulfonates. These are desirable because they can be made withrenewable, non-petroleum resources. Preparation of the alkyl estersulfonate surfactant component can be effected according to knownmethods disclosed in the technical literature. For instance, linearesters of C₈ -C₂₀ carboxylic acids can be sulfonated with gaseous SO₃according to "The Journal of the American Oil Chemists Society," 52(1975), pp 323-329 Suitable starting materials would include naturalfatty substances as derived from tallow, palm, and coconut oils, etc.

The preferred alkyl ester sulfonate surfactant, especially for laundryapplications, comprises alkyl ester sulfonate surfactants of thestructural formula: ##STR1## wherein R³ is a C₈ -C₂₀ hydrocarbyl,preferably an alkyl, or combination thereof, R⁴ is a C₁ -C₆ hydrocarbyl,preferably an alkyl, or combination thereof, and M is a solublesalt-forming cation. Suitable salts include metal salts such as sodium,potassium, and lithium salts, and substituted or unsubstituted ammoniumsalts, such as methyl-, dimethyl, -trimethyl, and quaternary ammoniumcations, e.g. tetramethyl-ammonium and dimethyl piperdinium, and cationsderived from alkanolamines, e.g. monoethanolamine, diethanolamine, andtriethanolamine. Preferably, R³ is C₁₀ -C₁₆ alkyl, and R⁴ is methyl,ethyl or isopropyl. Especially preferred are the methyl ester sulfonateswherein R³ is C₁₄ -C₁₆ alkyl.

Alkyl sulfate surfactants are another type of anionic surfactant ofimportance for use herein. In addition to providing excellent overallcleaning ability when used in combination with polyhydroxy fatty acidamides (see below), including good grease/oil cleaning over a wide rangeof temperatures, wash concentrations, and wash times, dissolution ofalkyl sulfates can be obtained, as well as improved formulability inliquid detergent formulations are water soluble salts or acids of theformula ROSO₃ M wherein R preferably is a C₁₀ -C₂₄ hydrocarbyl,preferably an alkyl or hydroxyalkyl having a C₁₀ -C₂₀ alkyl component,more preferably a C₁₂ -C₁₈ alkyl or hydroxyalkyl, and M is H or acation, e.g., an alkali metal cation (e.g., sodium, potassium, lithium),substituted or unsubstituted ammonium cations such as methyl-,dimethyl-, and trimethyl ammonium and quaternary ammonium cations, e.g.,tetramethyl-ammonium and dimethyl piperidinium, and cations derived fromalkanolamines such as ethanolamine, diethanolamine, triethanolamine, andmixtures thereof, and the like. Typically, alkyl chains of C₁₂₋₁₆ arepreferred for lower wash temperatures (e.g., below about 50° C.) andC₁₆₋₁₈ alkyl chains are preferred for higher wash temperatures (e.g.,above about 50° C.).

Alkyl alkoxylated sulfate surfactants are another category of usefulanionic surfactant. These surfactants are water soluble salts or acidstypically of the formula RO(A)_(m) SO₃ M wherein R is an unsubstitutedC₁₀ -C₂₄ alkyl or hydroxyalkyl group having a C₁₀ -C₂₄ alkyl component,preferably a C₁₂ -C₂₀ alkyl or hydroxyalkyl, more preferably C₁₂ -C₁₈alkyl or hydroxyalkyl, A is an ethoxy or propoxy unit, m is greater thanzero, typically between about 0.5 and about 6, more preferably betweenabout 0.5 and about 3, and M is H or a cation which can be, for example,a metal cation (e.g., sodium, potassium, lithium, calcium, magnesium,etc.), ammonium or substituted-ammonium cation. Alkyl ethoxylatedsulfates as well as alkyl propoxylated sulfates are contemplated herein.Specific examples of substituted ammonium cations include methyl-,dimethyl-, trimethyl-ammonium and quaternary ammonium cations, such astetramethyl-ammonium, dimethyl piperidinium and cations derived fromalkanolamines, e.g. monoethanolamine, diethanolamine, andtriethanolamine, and mixtures thereof. Exemplary surfactants are C₁₂-C₁₈ alkyl polyethoxylate (1.0) sulfate, C₁₂ -C₁₈ alkyl polyethoxylate(2.25) sulfate, C₁₂ -C₁₈ alkyl polyethoxylate (3.0) sulfate, and C₁₂-C₁₈ alkyl polyethoxylate (4.0) sulfate wherein M is convenientlyselected from sodium and potassium.

Other Anionic Surfactants

Other anionic surfactants useful for detersive purposes can also beincluded in the compositions hereof. These can include salts (including,for example, sodium, potassium, ammonium, and substituted ammonium saltssuch as mono-, di- and triethanolamine salts) of soap, C₉ -C₂₀ linearalkylbenzenesulphonates, C₈ -C₂₂ primary or secondary alkanesulphonates,C₈ -C₂₄ olefinsulphonates, sulphonated polycarboxylic acids prepared bysulphonation of the pyrolyzed product of alkaline earth metal citrates,e.g., as described in British patent specification No. 1,082,179, alkylglycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleylglycerol sulfates, alkyl phenol ethylene oxide ether sulfates, paraffinsulfonates, alkyl phosphates, isothionates such as the acylisothionates, N-acyl taurates, fatty acid amides of methyl tauride,alkyl succinamates and sulfosuccinates, monoesters of sulfosuccinate(especially saturated and unsaturated C₁₂ -C₁₈ monoesters) diesters ofsulfosuccinate (especially saturated and unsaturated C₆ -C₁₄ diesters),N-acyl sarcosinates, sulfates of alkylpolysaccharides such as thesulfates of alkylpolyglucoside (the nonionic nonsulfated compounds beingdescribed below), branched primary alkyl sulfates, alkyl polyethoxycarboxylates such as those of the formula RO(CH₂ CH₂ O)_(k) CH₂ COO--M⁺wherein R is a C₈ -C₂₂ alkyl, k is an integer from 0 to 10, and M is asoluble salt-forming cation, and fatty acids esterified with isethionicacid and neutralized with sodium hydroxide. Resin acids and hydrogenatedresin acids are also suitable, such as rosin, hydrogenated rosin, andresin acids and hydrogenated resin acids present in or derived from talloil. Further examples are given in "Surface Active Agents andDetergents" (Vol. I and II by Schwartz, Perry and Berch). A variety ofsuch surfactants are also generally disclosed in U.S. Pat. No.3,929,678, issued Dec. 30, 1975 to Laughlin, et al. at Column 23, line58 through Column 29, line 23 (herein incorporated by reference).

Nonionic Detergent Surfactants

Suitable nonionic detergent surfactants are generally disclosed in U.S.Pat. No. 3,929,678, Laughlin et al., issued Dec. 30, 1975, at column 13,line 14 through column 16, line 6, incorporated herein by reference.Exemplary, non-limiting classes of useful nonionic surfactants arelisted below.

1. The polyethylene, polypropylene, and polybutylene oxide condensatesof alkyl phenols. In general, the polyethylene oxide condensates arepreferred. These compounds include the condensation products of alkylphenols having an alkyl group containing from about 6 to about 12 carbonatoms in either a straight chain or branched chain configuration withthe alkylene oxide. In a preferred embodiment, the ethylene oxide ispresent in an amount equal to from about 5 to about 25 moles of ethyleneoxide per mole of alkyl phenol. Commercially available nonionicsurfactants of this type include Igepal® CO-630, marketed by the GAFCorporation; and Triton® X-45, X-114, X-100, and X-102, all marketed bythe Rohm & Haas Company. These compounds are commonly referred to asalkyl phenol alkoxylates, (e.g., alkyl phenol ethoxylates).

2. The condensation products of aliphatic alcohols with from about 1 toabout 25 moles of ethylene oxide. The alkyl chain of the aliphaticalcohol can either be straight or branched, primary or secondary, andgenerally contains from about 8 to about 22 carbon atoms. Particularlypreferred are the condensation products of alcohols having an alkylgroup containing from about 10 to about 20 carbon atoms with from about2 to about 18 moles of ethylene oxide per mole of alcohol. Examples ofcommercially available nonionic surfactants of this type includeTergitol® 15-S-9 (the condensation product of C₁₁ -C₁₅ linear secondaryalcohol with 9 moles ethylene oxide), Tergitol® 24-L-6 NMW (thecondensation product of C₁₂ -C₁₄ primary alcohol with 6 moles ethyleneoxide with a narrow molecular weight distribution), both marketed byUnion Carbide Corporation; Neodol® 45-9 (the condensation product of C₁₄-C₁₅ linear alcohol with 9 moles of ethylene oxide), Neodol® 23-6.5 (thecondensation product of C₁₂ -C₁₃ linear alcohol with 6.5 moles ofethylene oxide), Neodol® 45-7 (the condensation product of C₁₄ -C₁₅linear alcohol with 7 moles of ethylene oxide), Neodol® 45-4 (thecondensation product of C₁₄ -C₁₅ linear alcohol with 4 moles of ethyleneoxide), marketed by Shell Chemical Company, and Kyro® EOB (thecondensation product of C₁₃ -C₁₅ alcohol with 9 moles ethylene oxide),marketed by The Procter & Gamble Company. This category of nonionicsurfactant is referred to generally as "alkyl ethoxylates."

3. The condensation products of ethylene oxide with a hydrophobic baseformed by the condensation of propylene oxide with propylene glycol. Thehydrophobic portion of these compounds preferably has a molecular weightof from about 1500 to about 1800 and exhibits water insolubility. Theaddition of polyoxyethylene moieties to this hydrophobic portion tendsto increase the water solubility of the molecule as a whole, and theliquid character of the product is retained up to the point where thepolyoxyethylene content is about 50% of the total weight of thecondensation product, which corresponds to condensation with up to about40 moles of ethylene oxide. Examples of compounds of this type includecertain of the commercially-available Pluronic® surfactants, marketed byBASF.

4. The condensation products of ethylene oxide with the productresulting from the reaction of propylene oxide and ethylenediamine. Thehydrophobic moiety of these products consists of the reaction product ofethylenediamine and excess propylene oxide, and generally has amolecular weight of from about 2500 to about 3000. This hydrophobicmoiety is condensed with ethylene oxide to the extent that thecondensation product contains from about 40% to about 80% by weight ofpolyoxyethylene and has a molecular weight of from about 5,000 to about11,000. Examples of this type of nonionic surfactant include certain ofthe commercially available Tetronic® compounds, marketed by BASF.

5. Semi-polar nonionic surfactants are a special category of nonionicsurfactants which include water-soluble amine oxides containing onealkyl moiety of from about 10 to about 18 carbon atoms and 2 moietiesselected from the group consisting of alkyl groups and hydroxyalkylgroups containing from about 1 to about 3 carbon atoms; water-solublephosphine oxides containing one alkyl moiety of from about 10 to about18 carbon atoms and 2 moieties selected from the group consisting ofalkyl groups and hydroxyalkyl groups containing from about 1 to about 3carbon atoms; and water-soluble sulfoxides containing one alkyl moietyof from about 10 to about 18 carbon atoms and a moiety selected from thegroup consisting of alkyl and hydroxyalkyl moieties of from about 1 toabout 3 carbon atoms.

Semi-polar nonionic detergent surfactants include the amine oxidesurfactants having the formula ##STR2## wherein R³ is an alkyl,hydroxyalkyl, or alkyl phenyl group or mixtures thereof containing fromabout 8 to about 22 carbon atoms; R⁴ is an alkylene or hydroxyalkylenegroup containing from about 2 to about 3 carbon atoms or mixturesthereof; x is from 0 to about 3; and each R⁵ is an alkyl or hydroxyalkylgroup containing from about 1 to about 3 carbon atoms or a polyethyleneoxide group containing from about 1 to about 3 ethylene oxide groups.The R⁵ groups can be attached to each other, e.g., through an oxygen ornitrogen atom, to form a ring structure.

These amine oxide surfactants in particular include C₁₀ -C₁₈ alkyldimethyl amine oxides and C₈ -C₁₂ alkoxy ethyl dihydroxy ethyl amineoxides.

6. Alkylpolysaccharides disclosed in U.S. Pat. No. 4,565,647, Llenado,issued Jan. 21, 1986, having a hydrophobic group containing from about 6to about 30 carbon atoms, preferably from about 10 to about 16 carbonatoms and a polysaccharide, e.g., a polyglycoside, hydrophilic groupcontaining from about 1.3 to about 10, preferably from about 1.3 toabout 3, most preferably from about 1.3 to about 2.7 saccharide units.Any reducing saccharide containing 5 or 6 carbon atoms can be used,e.g., glucose, galactose and galactosyl moieties can be substituted forthe glucosyl moieties. (Optionally the hydrophobic group is attached atthe 2-, 3-, 4-, etc. positions thus giving a glucose or galactose asopposed to a glucoside or galactoside.) The intersaccharide bonds canbe, e.g., between the one position of the additional saccharide unitsand the 2-, 3-, 4-, and/or 6- positions on the preceding saccharideunits.

Optionally, and less desirably, there can be a polyalkylene-oxide chainjoining the hydrophobic moiety and the polysaccharide moiety. Thepreferred alkyleneoxide is ethylene oxide. Typical hydrophobic groupsinclude alkyl groups, either saturated or unsaturated, branched orunbranched containing from about 8 to about 18, preferably from about 10to about 16, carbon atoms. Preferably, the alkyl group is a straightchain saturated alkyl group. The alkyl group can contain up to about 3hydroxy groups and/or the polyalkyleneoxide chain can contain up toabout 10, preferably less than 5, alkyleneoxide moieties. Suitable alkylpolysaccharides are octyl, nonyl, decyl, undecyldodecyl, tridecyl,tetradecyl, pentadecyl, hexadecyl, heptadecyl, and octadecyl, di-, tri-,tetra-, penta-, and hexaglucosides, galactosides, lactosides, glucoses,fructosides, fructoses and/or galactoses. Suitable mixtures includecoconut alkyl, di-, tri-, tetra-, and pentaglucosides and tallow alkyltetra-, penta-, and hexa-glucosides.

The preferred alkylpolyglycosides have the formula

    R.sup.2 O(C.sub.n H.sub.2n O).sub.t (glycosyl).sub.x

wherein R² is selected from the group consisting of alkyl, alkyl-phenyl,hydroxyalkyl, hydroxyalkylphenyl, and mixtures thereof in which thealkyl groups contain .from about 10 to about 18, preferably from about12 to about 14, carbon atoms; n is 2 or 3, preferably 2; t is from 0 toabout 10, preferably 0; and x is from about 1.3 to about 10, preferablyfrom about 1.3 to about 3, most preferably from about 1.3 to about 2.7.The glycosyl is preferably derived from glucose. To prepare thesecompounds, the alcohol or alkylpolyethoxy alcohol is formed first andthen reacted with glucose, or a source of glucose, to form the glucoside(attachment at the 1-position). The additional glycosyl units can thenbe attached between their 1-position and the preceding glycosyl units2-, 3-, 4- and/or 6-position, preferably predominantly the 2-position.

7. Fatty acid amide surfactants having the formula: ##STR3## wherein R⁶is an alkyl group containing from about 7 to about 21 (preferably fromabout 9 to about 17) carbon atoms and each R⁷ is selected from the groupconsisting of hydrogen, C₁ -C₄ alkyl, C₁ -C₄ hydroxyalkyl, and --(C₂ H₄O)_(x) H where x varies from about 1 to about 3.

Preferred amides are C₈ -C₂₀ ammonia amides, monoethanolamides,diethanolamides, and isopropanolamides.

Cationic Surfactants

Cationic detersive surfactants can also be included in detergentcompositions of the present invention. Cationic surfactants include theammonium surfactants such as alkyldimethylammonium halogenides, andthose surfactants having the formula:

    [R.sup.2 (OR.sup.3).sub.y ][R.sup.4 (OR.sup.3).sub.y ].sub.2 R.sup.5 N.sup.+ X.sup.-

wherein R² is an alkyl or alkyl benzyl group having from about 8 toabout 18 carbon atoms in the alkyl chain, each R³ is selected from thegroup consisting of --CH₂ CH₂ --, --CH₂ CH(CH₃)--, --CH₂ CH(CH₂ OH)--,--CH₂ CH₂ CH₂ --, and mixtures thereof; each R⁴ is selected from thegroup consisting of C₁ -C₄ alkyl, C₁ -C₄ hydroxyalkyl, benzyl, ringstructures formed by joining the two R⁴ groups, --CH₂ CHOH--CHOHCOR⁶CHOHCH₂ OH wherein R⁶ is any hexose or hexose polymer having a molecularweight less than about 1000, and hydrogen when y is not 0; R⁵ is thesame as R⁴ or is an alkyl chain wherein the total number of carbon atomsof R² plus R⁵ is not more than about 18; each y is from 0 to about 10and the sum of the y values is from 0 to about 15; and X is anycompatible anion.

Other cationic surfactants useful herein are also described in U.S. Pat.No. 4,228,044, Cambre, issued Oct. 14, 1980, incorporated herein byreference.

Other Surfactants

Ampholytic surfactants can be incorporated into the detergentcompositions hereof. These surfactants can be broadly described asaliphatic derivatives of secondary or tertiary amines, or aliphaticderivatives of heterocyclic secondary and tertiary amines in which thealiphatic radical can be straight chain or branched. One of thealiphatic substituents contains at least about 8 carbon atoms, typicallyfrom about 8 to about 18 carbon atoms, and at least one contains ananionic water-solubilizing group, e.g., carboxy, sulfonate, sulfate. SeeU.S. Pat. No. 3,929,678 to Laughlin et al., issued Dec. 30, 1975 atcolumn 19, lines 18-35 (herein incorporated by reference) for examplesof ampholytic surfactants.

Zwitterionic surfactants can also be incorporated into the detergentcompositions hereof. These surfactants can be broadly described asderivatives of secondary and tertiary amines, derivatives ofheterocyclic secondary and tertiary amines, or derivatives of quaternaryammonium, quaternary phosphonium or tertiary sulfonium compounds. SeeU.S. Pat. No. 3,929,678 to Laughlin et al., issued Dec. 30, 1975 atcolumn 19, line 38 through column 22, line 48 (herein incorporated byreference) for examples of zwitterionic surfactants.

Ampholytic and zwitterionic surfactants are generally used incombination with one or more anionic and/or nonionic surfactants.

Polyhydroxy Fatty Acid Amide Surfactant

The liquid detergent compositions hereof may also contain an "enzymeperformance-enhancing amount" of polyhydroxy fatty acid amidesurfactant. By "enzyme-enhancing" is meant that the formulator of thecomposition can select an amount of polyhydroxy fatty acid amide to beincorporated into the compositions that will improve enzyme cleaningperformance of the detergent composition. In general, for conventionallevels of enzyme, the incorporation of about 1%, by weight, polyhydroxyfatty acid amide will enhance enzyme performance.

The detergent compositions hereof will typically comprise at least about1% weight basis, polyhydroxy fatty acid amide surfactant and preferablyat least from about 3% to about 50%, most preferably from about 3% to30%, of the polyhydroxy fatty acid amide.

The polyhydroxy fatty acid amide surfactant component comprisescompounds of the structural formula: ##STR4## wherein: R¹ is H, C₁ -C₄hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, or a mixture thereof,preferably C₁ -C₄ alkyl, more preferably C₁ or C₂ alkyl, most preferablyC₁ alkyl (i.e., methyl); and R² is a C₅ -C₃₁ hydrocarbyl, preferablystraight chain C₇ -C₁₉ alkyl or alkenyl, more preferably straight chainC₉ -C₁₇ alkyl or alkenyl, most preferably straight chain C₁₁ -C₁₅ alkylor alkenyl, or mixtures thereof; and Z is a polyhydroxyhydrocarbylhaving a linear hydrocarbyl chain with at least 3 hydroxyls directlyconnected to the chain, or an alkoxylated derivative (preferablyethoxylated or propoxylated) thereof. Z preferably will be derived froma reducing sugar in a reductive amination reaction; more preferably Zwill be a glycityl. Suitable reducing sugars include glucose, fructose,maltose, lactose, galactose, mannose, and xylose. As raw materials, highdextrose corn syrup, high fructose corn syrup, and high maltose cornsyrup can be utilized as well as the individual sugars listed above.These corn syrups may yield a mix of sugar components for Z. It shouldbe understood that it is by no means intended to exclude other suitableraw materials. Z preferably will be selected from the group consistingof --CH₂ --(CHOH)_(n) --CH₂ OH, --CH(CH₂ OH)--(CHOH)_(n-1) -- CH₂ OH,--CH₂ --(CHOH)₂ (CHOR')(CHOH)--CH₂ OH, and alkoxylated derivativesthereof, where n is an integer from 3 to 5, inclusive, and R' is H or acyclic or aliphatic monosaccharide. Most preferred are glycityls whereinn is 4, particularly --CH₂ --(CHOH)₄ --CH₂ OH.

In Formula (I), R' can be, for example, N-methyl, N-ethyl, N-propyl,N-isopropyl, N-butyl, N-2-hydroxy ethyl, or N-2-hydroxy propyl.

R2--CO--N< can be, for example, cocamide, stearamide, oleamide,lauramide, myristamide, capricamide, palmitamide, tallowamide, etc.

Z can be 1-deoxyglucityl, 2-deoxyfructityl, 1-deoxymaltityl,1-deoxylactityl, 1-deoxygalactityl, 1-deoxymannityl,1-deoxymaltotriotityl, etc.

Methods for making polyhydroxy fatty acid amides are known in the art.In general, they can be made by reacting an alkyl amine with a reducingsugar in a reductive amination reaction to form a corresponding N-alkylpolyhydroxyamine, and then reacting the N-alkyl polyhydroxyamine with afatty aliphatic ester or triglyceride in a condensation/amidation stepto form the N-alkyl, N-polyhydroxy fatty acid amide product. Processesfor making compositions containing polyhydroxy fatty acid amides aredisclosed, for example, in G.B. Patent Specification 809,060, publishedFeb. 18, 1959, by Thomas Hedley & Co., Ltd., U.S. Pat. No. 2,965,576,issued Dec. 20, 1960 to E. R. Wilson, and U.S. Pat. Nos. 2,703,798,Anthony M. Schwartz, issued Mar. 8, 1955, and 1,985,424, issued Dec. 25,1934 to Piggott, each of which is incorporated herein by reference.

D. Second Enzyme

Preferred compositions herein further comprise a performance-enhancingamount of a detergent-compatible second enzyme. By"detergent-compatible" is meant compatibility with the other ingredientsof a liquid detergent composition, such as detersive surfactant anddetergency builder. These second enzymes are preferably selected fromthe group consisting of lipase, amylase, cellulase, and mixturesthereof. The term "second enzyme" excludes the proteolytic enzymesdiscussed above, so each composition contains at least two kinds ofenzyme, including at least one proteolytic enzyme. The amount of secondenzyme used in the composition varies according to the type of enzyme.In general, from about 0.0001 to 0.3, more preferably 0.001 to 0.1,weight % of these second enzymes are preferably used. Mixtures of thesame class of enzymes (e.g. lipase) or two or more classes (e.g.cellulase and lipase) may be used. Purified or non-purified forms of theenzyme may be used.

Any lipolytic enzyme suitable for use in a liquid detergent compositioncan be used in these compositions. Suitable lipase enzymes for useherein include those of bacterial and fungal origin.

Suitable bacterial lipases include those produced by microorganisms ofthe Pseudomonas groups, such as Pseudomonas stutzeri ATCC 19.154, asdisclosed in British Patent 1,372,034, incorporated herein by reference.Suitable lipases include those which show a positive immunologicalcross-reaction with the antibody of the lipase produced by themicroorganism Pseudomonas fluorescens IAM 1057. This lipase and a methodfor its purification have been described in Japanese Patent Application53-20487, laid open on Feb. 24, 1978. This lipase is available fromAmano Pharmaceutical Co. Ltd., Nagoya, Japan, under the trade nameLipase P "Amano," hereinafter referred to as "Amano-P." Such lipasesshould show a positive immunological cross-reaction with the Amano-Pantibody, using the standard and well-known immunodiffusion procedureaccording to Ouchterlony (Acta. Med. Scan., 133, pages 76-79 (1950)).These lipases, and a method for their immunological cross-reaction withAmano-P, are also described in U.S. Pat. No. 4,707,291, Thom et al.,issued Nov. 17, 1987, incorporated herein by reference. Typical examplesthereof are the Amano-P lipase, the lipase ex Pseudomonas fragi FERM P1339 (available under the trade name Amano-B), lipase ex Pseudomonasnitroreducens var. lipolyticum FERM P 1338 (available under the tradename Amano-CES), lipases ex Chromobacter viscosum, e.g. Chromobacterviscosum var. lipolyticum NRRLB 3673, commercially available from ToyoJozo Co., Tagata, Japan; and further Chromobacter viscosum lipases fromU.S. Biochemical Corp., U.S.A. and Disoynth Co., The Netherlands, andlipases ex Pseudomonas gladioli.

Suitable fungal lipases include those producible by Humicola lanuginosaand Thermomyces lanuginosus. Most preferred is lipase obtained bycloning the gene from Humicola lanuginosa and expressing the gene inAspergillus oryzae as described in European Patent Application 0 258 068(Novo Industri A/S), commercially available from Novo Nordisk A/S underthe trade name Lipolase®.

From about 10 to 18000, preferably about 60 to 6000, lipase units pergram (LU/g) of lipase can be used in these compositions. A lipase unitis that amount of lipase which produces 1 mmol of titratable fatty acidper minute in a pH stat, where pH is 9.0, temperature is 30° C.,substrate is an emulsion of 3.3wt % of olive oil and 3.3% gum arabic, inthe presence of 13 mmol/l Ca⁺⁺ and 20 mmol/l NaCl in 5 mmol/lTris-buffer.

Any cellulase suitable for use in a liquid detergent composition can beused in these compositions. Suitable cellulase enzymes for use hereininclude those from bacterial and fungal origins. Preferably, they willhave a pH optimum of between 5 and 9.5. From about 0.0001 to 0.1 weight% cellulase can be used.

Suitable cellulases are disclosed in U.S. Pat. No. 4,435,307,Barbesgaard et al., issued Mar. 6, 1984, incorporated herein byreference, which discloses fungal cellulase produced from Humicolainsolens. Suitable cellulases are also disclosed in GB-A-2.075,028,GB-A-2,095,275 and DE-OS-2,247,832.

Examples of such cellulases are cellulases produced by a strain ofHumicola insolens (Humicola grisea var. thermoidea), particularly theHumicola strain DSM 1800, and cellulases produced by a fungus ofBacillus N or a cellulase 212-producing fungus belonging to the genusAeromonas, and cellulase extracted from the hepatopancreas of a marinemollusc (Dolabella Auricula Solander).

Any amylase suitable for use in a liquid detergent composition can beused in these compositions. Amylases include, for example, amylasesobtained from a special strain of B.licheniformis, described in moredetail in British Patent Specification No. 1,296,839 (Novo). Amylolyticproteins include, for example, Rapidase®, International Bio-Synthetics,Inc. and Termamyl® Novo Industries.

From about 0.0001% to 0.55, preferably 0.0005 to 0.1, wt. % amylase canbe used.

E. Optional Ingredients

Detergent builders can optionally be included in the compositionsherein. From 0 to about 50 weight % detergency builder can be usedherein. Inorganic as well as organic builders can be used. When present,the compositions will typically comprise at least about 1% builder.Liquid formulations preferably comprise from about 3% to 30%, morepreferably about 5 to 20%, by weight, of detergent builder.

Inorganic detergent builders include, but are not limited to, the alkalimetal, ammonium and alkanolammonium salts of polyphosphates (exemplifiedby the tripolyphosphates, pyrophosphates, and glassy polymericmeta-phosphates), phosphonates, phytic acid, silicates, carbonates(including bicarbonates and sesquicarbonates), sulphates, andaluminosilicates. Borate builders, as well as builders containingborate-forming materials that can produce borate under detergent storageor wash conditions (hereinafter, collectively "borate builders"), canalso be used. Preferably, non-borate builders are used in thecompositions of the invention intended for use at wash conditions lessthan about 50° C., especially less than about 40° C.

Examples of silicate builders are the alkali metal silicates,particularly those having a SiO₂ :Na₂ O ratio in the range 1.6:1 to3.2:1 and layered silicates, such as the layered sodium silicatesdescribed in U.S. Pat. No. 4,664,839, issued May 12, 1987 to H. P.Rieck, incorporated herein by reference. However, other silicates mayalso be useful such as for example magnesium silicate, which can serveas a crispening agent in granular formulations, as a stabilizing agentfor oxygen bleaches, and as a component of suds control systems.

Examples of carbonate builders are the alkaline earth and alkali metalcarbonates, including sodium carbonate and sesquicarbonate and mixturesthereof with ultra-fine calcium carbonate as disclosed in German PatentApplication No. 2,321,001 published on Nov. 15, 1973, the disclosure ofwhich is incorporated herein by reference.

Aluminosilicate builders are useful in the present invention.Aluminosilicate builders are of great importance in most currentlymarketed heavy duty granular detergent compositions, and can also be asignificant builder ingredient in liquid detergent formulations.Aluminosilicate builders include those having the empirical formula:

    M.sub.z (zAlO.sub.2 ·ySiO.sub.2)

wherein M is sodium, potassium, ammonium or substituted ammonium, z isfrom about 0.5 to about 2; and y is 1; this material having a magnesiumion exchange capacity of at least about 50 milligram equivalents ofCaCO₃ hardness per gram of anhydrous aluminosilicate. Preferredalumino-silicates are zeolite builders which have the formula:

    Na.sub.z [(AlO.sub.2).sub.z (SiO.sub.2).sub.y ]·xH.sub.2 O

wherein z and y are integers of at least 6, the molar ratio of z to y isin the range from 1.0 to about 0.5, and x is an integer from about 15 toabout 264.

Useful aluminosilicate ion exchange materials are commerciallyavailable. These aluminosilicates can be crystalline or amorphous instructure and can be naturally-occurring aluminosilicates orsynthetically derived. A method for producing aluminosilicate ionexchange materials is disclosed in U.S. Pat. No. 3,985,669, Krummel, etal., issued Oct. 12, 1976, incorporated herein by reference. Preferredsynthetic crystalline aluminosilicate ion exchange materials usefulherein are available under the designations Zeolite A, Zeolite P (B),and Zeolite X. In an especially preferred embodiment, the crystallinealuminosilicate ion exchange material has the formula:

    Na.sub.12 [(AlO.sub.2).sub.12 (SiO.sub.2).sub.12 ]·xH.sub.2 O

wherein x is from about 20 to about 30, especially about 27. Thismaterial is known as Zeolite A. Preferably, the aluminosilicate has aparticle size of about 0.1-10 microns in diameter.

Specific examples of polyphosphates are the alkali metaltripolyphosphates, sodium, potassium and ammonium pyrophosphate, sodiumand potassium and ammonium pyrophosphate, sodium and potassiumorthophosphate, sodium polymeta phosphate in which the degree ofpolymerization ranges from about 6 to about 21, and salts of phyticacid.

Examples of phosphonate builder salts are the water-soluble salts ofethane 1-hydroxy-1,1-diphosphonate particularly the sodium and potassiumsalts, the water-soluble salts of methylene diphosphonic acid e.g. thetrisodium and tripotassium salts and the water-soluble salts ofsubstituted methylene diphosphonic acids, such as the trisodium andtripotassium ethylidene, isopyropylidene benzylmethylidene and halomethylidene phosphonates. Phosphonate builder salts of theaforementioned types are disclosed in U.S. Pat. Nos. 3,159,581 and3,213,030 issued Dec. 1, 1964 and Oct. 19, 1965, to Diehl; 3,422,021issued Jan. 14, 1969, to Roy; and 3,400,148 and 3,422,137 issued Sep. 3,1968, and Jan. 14, 1969 to Quimby, said disclosures being incorporatedherein by reference.

Organic detergent builders preferred for the purposes of the presentinvention include a wide variety of polycarboxylate compounds. As usedherein, "polycarboxylate" refers to compounds having a plurality ofcarboxylate groups, preferably at least 3 carboxylates.

Polycarboxylate builder can generally be added to the composition inacid form, but can also be added in the form of a neutralized salt. Whenutilized in salt form, alkali metals, such as sodium, potassium, andlithium, or alkanolammonium salts are preferred.

Included among the polycarboxylate builders are a variety of categoriesof useful materials. One important category of polycarboxylate buildersencompasses the ether polycarboxylates. A number of etherpolycarboxylates have been disclosed for use as detergent builders.Examples of useful ether polycarboxylates include oxydisuccinate, asdisclosed in Berg, U.S. Pat. Nos. 3,128,287, issued Apr. 7, 1964, andLamberti et al., 3,635,830, issued Jan. 18, 1972, both of which areincorporated herein by reference.

A specific type of ether polycarboxylates useful as builders in thepresent invention also include those having the general formula:

    CH(A)(COOX)--CH(COOX)--O--CH(COOX)--CH(COOX)(B)

wherein A is H or OH; B is H or --O--CH(COOX)--CH₂ (COOX); and X is H ora salt-forming cation. For example, if in the above general formula Aand B are both H, then the compound is oxydissuccinic acid and itswater-soluble salts. If A is OH and B is H, then the compound istartrate monosuccinic acid (TMS) and its water-soluble salts. If A is Hand B is --O--CH(COOX)--CH₂ (COOX), then the compound is tartratedisuccinic acid (TDS) and its water-soluble salts. Mixtures of thesebuilders are especially preferred for use herein. Particularly preferredare mixtures of TMS and TDS in a weight ratio of TMS to TDS of fromabout 97:3 to about 20:80. These builders are disclosed in U.S. Pat. No.4,663,071, issued to Bush et al., on May 5, 1987.

Suitable ether polycarboxylates also include cyclic compounds,particularly alicyclic compounds, such as those described in U.S. Pat.Nos. 3,923,679; 3,835,163; 4,158,635; 4,120,874 and 4,102,903, all ofwhich are incorporated herein by reference.

Other useful detergency builders include the etherhydroxypolycarboxylates represented by the structure:

    HO--[C(R)(COOM)--C(R)(COOM)--O].sub.n --H

wherein M is hydrogen or a cation wherein the resultant salt iswater-soluble, preferably an alkali metal, ammonium or substitutedammonium cation, n is from about 2 to about 15 (preferably n is fromabout 2 to about 10, more preferably n averages from about 2 to about 4)and each R is the same or different and selected from hydrogen, C₁₋₄alkyl or C₁₋₄ substituted alkyl (preferably R is hydrogen).

Still other ether polycarboxylates include copolymers of maleicanhydride with ethylene or vinyl methyl ether, 1,3,5-trihydroxybenzene-2,4,6-trisulphonic acid, and carboxymethyloxysuccinic acid.

Organic polycarboxylate builders also include the various alkali metal,ammonium and substituted ammonium salts of polyacetic acids. Examplesinclude the sodium, potassium, lithium, ammonium and substitutedammonium salts of ethylenediamine tetraacetic acid, and nitrilotriaceticacid.

Also included are polycarboxylates such as mellitic acid, succinic acid,oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid,and carboxymethyloxysuccinic acid, and soluble salts thereof.

Citrate builders, e.g., citric acid and soluble salts thereof(particularly sodium salt), are polycarboxylate builders of particularimportance for heavy duty liquid detergent formulations, but can also beused in granular compositions.

Other carboxylate builders include the carboxylated carbohydratesdisclosed in U.S. Pat. No. 3,723,322, Diehl, issued Mar. 28, 1973,incorporated herein by reference.

Also suitable in the detergent compositions of the present invention arethe 3,3-dicarboxy-4-oxa-1,6-hexanedioates and the related compoundsdisclosed in U.S. Pat. No. 4,566,984, Bush, issued Jan. 28, 1986,incorporated herein by reference. Useful succinic acid builders includethe C₅ -C₂₀ alkyl succinic acids and salts thereof. A particularlypreferred compound of this type is dodecenylsuccinic acid. Alkylsuccinic acids typically are of the general formula R--CH(COOH)CH₂(COOH) i.e., derivatives of succinic acid, wherein R is hydrocarbon,e.g., C₁₀ -C₂₀ alkyl or alkenyl, preferably C₁₂ -C₁₆ or wherein R may besubstituted with hydroxyl, sulfo, sulfoxy or sulfone substituents, allas described in the above-mentioned patents.

The succinate builders are preferably used in the form of theirwater-soluble salts, including the sodium, potassium, ammonium andalkanolammonium salts.

Specific examples of succinate builders include: laurylsuccinate,myristylsuccinate, palmitylsuccinate, 2-dodecenylsuccinate (preferred),2-pentadecenylsuccinate, and the like. Laurylsuccinates are thepreferred builders of this group, and are described in European PatentApplication 86200690.5/0,200,263, published Nov. 5, 1986.

Examples of useful builders also include sodium and potassiumcarboxymethyloxymalonate, carboxymethyloxysuccinate,cis-cyclo-hexane-hexacarboxylate, cis-cyclopentanetetracarboxylate,water-soluble polyacrylates (these polyacrylates having molecularweights to above about 2,000 can also be effectively utilized asdispersants), and the copolymers of maleic anhydride with vinyl methylether or ethylene.

Other suitable polycarboxylates are the polyacetal carboxylatesdisclosed in U.S. Pat. No. 4,144,226, Crutchfield et al., issued Mar.13, 1979, incorporated herein by reference. These polyacetalcarboxylates can be prepared by bringing together, under polymerizationconditions, an ester of glyoxylic acid and a polymerization initiator.The resulting polyacetal carboxylate ester is then attached tochemically stable end groups to stabilize the polyacetal carboxylateagainst rapid depolymerization in alkaline solution, converted to thecorresponding salt, and added to a surfactant.

Polycarboxylate builders are also disclosed in U.S. Pat. No. 3,308,067,Diehl, issued Mar. 7, 1967, incorporated herein by reference. Suchmaterials include the water-soluble salts of homo- and copolymers ofaliphatic carboxylic acids such as maleic acid, itaconic acid andmethylenemalonic acid. Other organic builders known in the art can alsobe used. For example, monocarboxylic acids, and soluble salts thereof,having long chain hydrocarbyls can be utilized. These would includematerials generally referred to as "soaps." Chain lengths of C₁₀ -C₂₀are typically utilized. The hydrocarbyls can be saturated orunsaturated.

Other optional ingredients include soil release agents, chelatingagents, clay soil removal/anti redeposition agents, polymeric dispersingagents, bleaches, brighteners, suds suppresors, solvents and aestheticagents.

The detergent composition herein can be formulated as a variety ofcompositions, for instance as laundry detergents as well as hard surfacecleaners or dishwashing compositions.

The compositions according to the present invention are furtherillustrated by the following examples.

EXAMPLES

Example A:

The following compositions were made by lmixing the listed ingredientsin the listed proportions. In the examples hereinafter, the peptidetrifluoromethyl ketones which were used were:

Peptide trifluoromethyl ketone 1: CH₃ O--(O) C-Phe-Gly-Ala-LeuCF₃

Peptide trifluoromethyl ketone 2: CH₃ N--(O) C-Phe-Gly-Ala-LeuCF₃

Peptide trifluoromethyl ketone 3: CH₃ O--(O) C-Phe-Gly-Ala-PheCF₃

Peptide trifluoromethyl ketone 4: CH₃ N--(O) C-Phe-Gly-Ala-PheCF₃

    __________________________________________________________________________    Compositions 1   2   3   4   5   6                                            __________________________________________________________________________    Linear alkyl benzene                                                                       8.5 15  6.5 10  12.5                                                                              4                                            sulfonic acid                                                                 Sodium C.sub.12-15 alkyl sulfate                                                           1   2   1   2   0   0                                            C.sub.14-15 alkyl 2.5 times                                                                10  5   10.5                                                                              0   11  9                                            ethoxylated sulfate                                                           C.sub.12 glucose amide                                                                     0   0   9   0   0   5                                            C.sub.12-15 alcohol 7 times                                                                3   10  4   7   2.5 0                                            ethoxylated                                                                   Fatty acid   2   5   5   4   2   2                                            Citric acid  5   6   7   4   6   4                                            C.sub.12-14 alkenyl substituted                                                            0   6   0   5   0   6                                            succinic acid                                                                 Sodium Hydroxide                                                                           2   6   2   4   1   1.5                                          Ethanol      2   1.5 2   4   2   1.5                                          Monoethanolamine                                                                           6   5   4   0   0   0                                            1,2-propane diol                                                                           12  10  5   5   4   6                                            Amylase (143 KNU/g)                                                                        0.1 0   0.1 0   0   0.1                                          Lipolase ® (100 KLU/g                                                                  0.3 0.2 0.5 0.5 0.3 0                                            commercial solution                                                           Protease B (34 g/L                                                                         0   0.8 1.5 0   0.5                                              commercial solution)                                                          Savinase ® (Commercial                                                                 0.4 0   0   0.5     0.6                                          solution)                                                                     Carezyme ®                                                                             0.5 1   0.8 0   0.2 0.8                                          (Experimental sample)                                                         Peptide trifluoromethyl                                                                    0.0075                                                                            --  --  --  0.0009                                                                            --                                           ketone 1                                                                      Peptide trifluoromethyl                                                                    --  0.005                                                                             --  --  --  --                                           ketone 2                                                                      Peptide trifluoromethyl                                                                    --  --  0.0001                                                                            --  --  0.008                                        ketone 3                                                                      Peptide trifluoromethyl                                                                    --  --  --  0.005                                                                             --  --                                           ketone 4                                                                      Water and minors                                                                           Balance to 100%                                                  __________________________________________________________________________

Example B:

CH₃ O--(O)C-Phe-Gly-Ala-Leu(trifluoromethyl) is synthesized according toScheme A. Other peptide trifuoromethyl ketones can be prepared byroutine adjustements. In scheme A, some of the intermediates arepurchased and where this is the case it has been noted in the Scheme.CF₃ TMS is synthesized according to the procedure of Prakash, J. Org.Chem., 1991, 56, 984. Dess-Martin Periodinane is synthesized accordingto the procedure of Martin, J. Org. Chem., 1983, 48, 4155.

N-trityl-leucine methyl ester (2)--To a solution of 2.50 g (13.8 mmol)of Leu-OMe.HCl in 100 ml CH₂ C₁₂ was added 3.86 ml TEA (27.5 mmol)dropwise. After the addition was complete 3.76 g (13.5 mmol) oftriphenylmethyl chloride in 15 ml CH₂ C1₂ was added dropwise. Themixture was stirred for 4 h. The solution was diluted with 5%EtOAc/petroleum ether and washed with water. The organic phase was dried(MgSO₄), filtered and the solvent removed. The residue waschromatographed on silica to give 4.8 g of pure product (90% yield).

N-trityl-leucinal (3)--To a cold (0°) solution of 4.70 g (12.2 mmol) ofN-trityl-leucine methyl ester in 100 ml THF was added 28.1 ml of a 1.5Msolution of diisobutylaluminum hydride (42.2 mmol) in THF dropwise. Thesolution was stirred for 6 h at this temperature and the reactionquenched with saturated Na-K tartrate, extracted with EtOac, dried(MgSO₄), filtered and the solvent removed. Recovered 4.13 g of thedesired material that was used without purification. To a solution of1.29 g (14.9 mmol) of oxalyl chloride in 30 ml CH₂ Cl₂ at -78° C. wasadded 2.26 ml DMSO (29.8 mmol) in 5 ml CH₂ Cl₂ dropwise. After theaddition was complete, 4.13 g (11.5 mmol) of crude N-tritylleucinol in10 ml CH₂ Cl₂ was added. The solution was stirred at this temperaturefor 0.5 h and 2.78 ml (19.9 mmol) of TEA was added. The solution waswarmed to 0° C. and poured into a mixture of water and ether. Theorganic phase was washed successively with 1N HCl, saturated NaHCO₃, andbrine. The solution was dried (MgSO₄), filtered and the solvent removedto afford 1.37 g of the desired compound.

5-Methyl-3-tritylamino-1,1,1-trifluoro-2-hexanol (4)--To a solution of1.37 g (3.83 mmol) of N-trityl-leucinal and 0.653 ml (4.59 mmol) of CF₃TMS in THF was added 0.121 g (0.383 mmol) of tetrabutylammonium fluoridetrihydrate in one portion. The solution was stirred for 3 h at roomtemperature and the solvent removed. The residue was dissolved in EtOAc,washed with water, dried (MgSO₄), and the solvent removed to afford 1.20g of product that was chromatographed on silica. Recovered 0.760 g pureproduct.

3-(N-CBz-Gly-Ala)-5-methyl-1,1,1-trifluoro-2-hexanol (5)--To a solutionof 1.21 g (2.83 mmol) of5-methyl-3-tritylamino-1,1,1,-trifluoro-2-hexanol in 10 ml dioxane wasadded 5 ml of 4.0M HCl in dioxane. The solution was stirred for 2 h atroom temperature and the solvent removed. The residue was trituratedwith ether and the solid material filtered. The resulting HCl salt(0.627 g, 2.83 mmol) was suspended in 10 ml CH₂ Cl₂ and Z-Gly-Ala-OHadded (0.793 g, 2.83 mmol). To this mixture was added 0.870 ml (6.23mmol) of TEA followed immediately by the addition of 0.473 ml (3.12mmol) of DECP. The mixture was stirred overnight and the solventremoved. The residue was dissolved in EtOAc and washed with 1N HCl,saturated NaHCO₃, and brine. The solution of product was dried (MgSO₄),filtered and the solvent removed to give 1.06 g product.

3-(N-Moc-Phe-Gly-Ala)-5-methyl-1,1,1-trifluoro-2-hexanol (6)--To asolution of 1.06 g (2.37 mmol) of3-(N-CBz-Gly-Ala)-5-methyl-1,1,1-trifluoro-2-hexanol in 5 ml MeOH wasadded 0.35 g Pd/C. The slurry was degassed and hydrogenated under apositive pressure of hydrogen overnight. The slurry was filtered throughCelite and the solvent removed. The residue was dissolved in CH₂ Cl₂ and0.528 g (2.37 mmol) of Moc-Phe-OH added. To this mixture was added 0.732ml (5.22 mmol) of TEA, followed by the addition of 0.395 ml (2.61 mmol)of DECP. The solution was stirred overnight and the solvent removed. Theresidue was chromatographed on silica to afford 0.720 g pure product.

3-(N-Moc-Phe-Gly-Ala)-5-methyl-1,1,1,-trifluoro-2-hexanone (7)--To aslurry of 1.59 g (3.75 mmol) of Dess-Martin periodinane in 15 ml CH₂ Cl₂was added 0.650 g (1.25 mmol) of3-(Moc-Phe-Gly-Ala)-5-methyl-1,1,1,-trifluoro-2-hexanol in 5 ml CH₂ Cl₂and the slurry stirred for 3 h. To this mixture was added 6.51 g (25.2mmol) of Na₂ S₂ O₃ in saturated NaHCO₃ and the resulting solutionstirred for 10 min. The solution was extracted with EtOAc and theorganic phase dried (MgSO₄), filtered, and the solvent removed. Theresidue was chromatographed on silica to afford 0.445 g of pure product.

Moc-Phe-OH (9)--L-Phenylalanine (5.0 g, 30.2 mmol) was dissolved in 30ml 1N NaOH and cooled to 0° C. Methyl chloroformate (2.53 ml, 31.8 mmol)was added dropwise while in a separate addition funnel 30 ml of 1N NaOHwas added simultaneously. After addition was complete the solution waswashed with 200 ml EtOAc and the aqueous phase acidified to pH=2. Themixture was extracted with EtOAc (2X 100 ml), dried (MgSO₄), filtered,and the solvent removed to afford 6.0 g product. ¹³ C NMR (CDCl₃) 37.75,52.57, 54.64, 128.63, 129.35, 135.74, 156.77, 175.76.

Phe=phenylalanine Pd/c=palladium on carbon CBz=carbobenzy/oxyGly=glycine Ala=alanine DECP=diethyl cyanophosphonate TEA=triethylamineMoc=methoxycarbonyl trityl=triphenylmethyl ##STR5##

What is claimed is:
 1. A liquid aqueous detergent compositioncomprising: (a) from 1% to 80% of a detersive surfactant;(b) from0.0001% to 1.0% of active proteolytic enzyme or mixtures thereof; and(c) from 0.00001% to 5% of a peptide trifluoromethyl ketone comprising 2or 3 amino acids and a C terminal end trifluoromethyl ketone of an aminoacid.
 2. The liquid aqueous detergent composition according to claim 1wherein the peptide trifluoromethyl ketone is selected fromtrifluoromethyl ketones having 2 or 3 amino acids wherein the C terminalend is selected from Ala-Leu(trifuoromethyl) andAla-Phe(trifuoromethyl).
 3. The liquid aqueous detergent compositionaccording to claim 2 wherein the peptide trifluoromethyl ketone isselected from Phe-Gly-Ala-Leu(trifluoromethyl),Phe-Gly-Ala-Phe(trifluoromethyl), and the N-terminal end protectedcarbamate or urea thereof.
 4. The liquid aqueous detergent compositionaccording to claim 1 wherein the proteolytic enzyme is selected fromsubtilisin-type protease.
 5. The liquid aqueous detergent compositionaccording to claim 2 wherein the proteolytic enzyme is selected fromsubtilisin-type protease.
 6. The liquid aqueous detergent compositionaccording to claim 3 wherein the proteolytic enzyme is selected fromsubtilisin-type protease.